Overview In this role you drive quality-driven clinical monitoring for investigator sites, ensuring studies run per protocol and regulatory standards. You work closely with sponsors and cross-functional teams, coordinating start-up, initiat...Read More>>.

Overview In this role you will support the advancement of clinical development by conducting on-site monitoring and oversight of trial activities. You’ll collaborate with sites to ensure protocol adherence, data integrity, and regulatory...Read More>>.

Overview As a CRA at Parexel, you will go beyond traditional monitoring to safeguard patient wellbeing and ensure study success across UK sites. You’ll manage site relationships, oversee quality from site identification to close-out, and...Read More>>.

Overview In this evergreen role, you contribute to a closely aligned sponsor partnership within a collaborative, quality-driven environment. You will monitor and support clinical studies at investigative sites, ensuring compliance with prot...Read More>>.

Overview In this role you drive global non-interventional studies as a Senior Lead CRA, guiding cross-country teams to ensure high-quality site management and compliance. You collaborate with Sponsors, PMs, and regulators to advance study s...Read More>>.

Overview In this role you support the execution of interventional studies as a Clinical Research Associate within IQVIA's sponsor-dedicated team. You will conduct on-site monitoring and ensure compliance with GCP/ICH while collaborating wit...Read More>>.

Overview In this role you drive site monitoring across interventional studies, ensuring GCP/ICH compliance and high-quality data. You collaborate with sites to optimize subject recruitment and manage study documentation. You’ll track regu...Read More>>.

Overview You will support and oversee clinical studies from a home-based role in the UK or Northern Ireland, ensuring studies are conducted to protocol, SOPs, and ICH-GCP standards. You will coordinate study setup and monitoring activities,...Read More>>.

Overview As a Clinical Research Associate in Abbott Diabetes Care, you contribute to advancing diabetes care through clinical studies supporting innovative medical technologies. You’ll join a collaborative Clinical Affairs team in Witney,...Read More>>.

Overview In this role you will monitor clinical studies across investigative sites, ensuring adherence to protocol, SOPs, ICH-GCP, and applicable regulations. You will coordinate study setup and monitoring activities, including investigator...Read More>>.

Research Associate (SB13960) - Bath, BA2 7AYAbout the roleAdvance Your Engineering Career Through Innovation and ImpactThe...Read More>>.

Research Associate in Spectroscopy and Molecular Modelling for Zeolite Catalysed Alcohol-to-jet-fuel Catalysis (SS13564R) - Bath, BA2 7AYAbout the roleThis role is part of the UK Catalysis Hub where the practical...Read More>>.

Research Associate/Fellow in Engineered Silk Manufacturing and Optical Fibre Technologies (SS13969) - Bath, BA2 7AYAbout the roleJoin the HOLLOW SILK project, an ambitious research project funded b...Read More>>.

Research Associate (SS13981) - Bath, BA2 7AYAbout the roleThe role is associated with the Royal Society International Collaboration Award “Operator learning for gradient flows with applications in imaging” led b...Read More>>.

Postdoctoral Research Associate (SS13987) - Bath, BA2 7AYThe Department of Mathematical Sciences at the University of Bath welcomes applications for an EPSRC-funded Research Associate in Analysis to work with Dr Matthew Schrecker in nonl...Read More>>.

Research associate in number theory (SS13993) - Bath, BA2 7AYAbout the roleApplications are invited for a postdoctoral research associate to work with Prof. Daniel Loughran as part of the EPSRC-funded programme gran...Read More>>.

IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP. You will coordinate monitoring visits, support recruitment plans, and ensure regulatory complian...Read More>>.

Our Clinical Operations (multi-sponsor) team in the UK is looking for a passionate CRA I with at least 6 months of independent monitoring experience to work across a diverse range of therapeutic areas – including Hematology/Oncology and Ophthalm...Read More>>.

IQVIA UK invites applications for Clinical Research Associates (CRAs) to join our Site Management team in Manchester. You will conduct site monitoring visits, support recruitment plans, ensure GCP/ICH compliance, and maintain TMF documentation....Read More>>.

IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor and manage study sites, ensuring adherence to protocol, GCP/ICH guidelines, and regulatory requirements. The role involves site visits, recruitment support, trai...Read More>>.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therap...Read More>>.

Syneos Health is seeking a Senior Clinical Research Associate with UK monitoring experience to oversee site qualification, initiation, monitoring and close-out visits, ensuring GCP compliance and patient safety across trials. The role requires up...Read More>>.

IQVIA is seeking an experienced Senior Clinical Research Associate to monitor and manage sites in the UK, ensuring protocol compliance and data quality. You will perform site visits, train sites, and collaborate with study teams to keep projects o...Read More>>.

The Cambridge-GSK Translational Immunology Collaboration (CG-TIC) invites applications for a Research Associate (Honorary Resident Doctor) based in the Department of Medicine, Cambridge. You will conduct high-quality clinical and laboratory studie...Read More>>.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions...Read More>>.

Abbott in the United Kingdom is seeking a Clinical Research Associate to support the delivery of clinical studies, ensuring activities align with study protocols, GCP, SOPs and regulatory requirements.You will develop relationships with cli...Read More>>.

IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor trials and ensure sites conduct studies according to the protocol and regulatory requirements. The role involves site visits, recruitment tracking, protocol trai...Read More>>.

Norwich Clinical Trials Unit at the University of East Anglia is seeking a Research Associate to support high-quality clinical statistics delivery within the Norwich Clinical Trials Unit.The role involves working with a Senior Statistician...Read More>>.

R&D Partners is seeking a Clinical Research Associate to coordinate and oversee clinical studies in the UK. You will act as the primary contact for study sites, support site activation, and collaborate with cross-functional teams to ensure success...Read More>>.

Are you ready to drive the future of clinical research? Looking to be in the heart of a company where precision meets purpose? R&D Partners is seeking a Clinical Research Associate to join our team. In this role, you will coordinate and ove...Read More>>.

Abbott in the United Kingdom is seeking a Clinical Research Associate to support the delivery of clinical studies, ensuring compliant conduct, documentation and reporting in line with GCP, SOPs, and regulatory requirements.You will develop...Read More>>.

IQVIA LLC is seeking an on-site Clinical Research Associate to monitor trial sites, ensure protocol compliance and maintain regulatory documentation. The role involves coordinating site activation, ongoing monitoring, and data query resolution acr...Read More>>.

IQVIA is seeking an on-site Clinical Research Associate to support site monitoring across multiple sites in the United Kingdom. You will conduct monitoring visits, ensure GCP compliance, and manage essential trial documentation with the study team...Read More>>.

Northampton General Hospital NHS Trust is seeking an experienced Senior Research Nurse (Band 6) for a part-time role (28 hours/week) to lead and deliver high-quality clinical research across NGH. You will manage a portfolio of studies, ensure comp...Read More>>.

IQVIA LLC is seeking an on-site monitoring professional to ensure adherence to GCP and protocol requirements across multiple sites. You will manage site communications, training, and issue resolution while tracking regulatory submissions and data...Read More>>.

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)...Read More>>.

Main area Clinical Research Nurse or Practitioner - Cardiac/Renal/Metabolic Grade Band 6 Contract Fixed term: 12 months (Newly created 12M contract) Hours Full time - 37.5 hours per week Job ref 200-7880759-GO-SC-A Site St George's Hospital...Read More>>.

IQVIA LLC is seeking experienced Clinical Research Associates in the UK to monitor study sites and manage site activities in line with the protocol and regulatory requirements.Responsibilities include site visits, regulatory tracking, and m...Read More>>.

Are you looking to build a career as a Clinical Research Associate within a specialist clinical research environment where you can develop your expertise, gain greater autonomy, and make a genuine impact? Our client is a privately owned, sp...Read More>>.

RBW Consulting in London seeks a Clinical Research Associate to join a specialist CRO environment. You will monitor studies, ensure compliance with GCP, and support site management with investigators and staff.The role offers focused work w...Read More>>.

The post holder will be responsible for the co-ordination and management of an interventional clinical trials covering mainly the Cardiac-Renal-Metabolic research portfolio at St George's. The post holder will work collaboratively with the...Read More>>.

Location:Leeds - Chapel Allerton HospitalContract Type:Fixed Term (Available for 24 months to complete a specific task or time limited work, including the need for specific expertise or additional resource for a project.)...Read More>>.

A diverse range of clinical research trials are in progress & following training, the post holder will participate in these studies as a co-/sub-investigator. These include Phase I trials of small molecule inhibitors, combination / multi-modality...Read More>>.

City St George’s, University of London is the University of business, practice and the professions and brings together the expertise and excellence of City, University of London and St George’s, University of London into one institution....Read More>>.

Clinical Research Nurse – Band 6 – HIV Research We are looking for a motivated and enthusiastic nurse to join the HIV Research Team at the Harrison Wing, Guy's and St Thomas Foundation Trust. The successful candidate will...Read More>>.

Job OverviewAn exciting opportunity has arisen for a Clinical Research Officer Band 5 to work as part of the Health and Care Research Wales Research and Development team in the BCUHB.Job OverviewAn exci...Read More>>.

Guy's and St Thomas NHS Foundation Trust is seeking a Clinical Research Nurse – Band 6 to join the HIV Research Team. The role supports the HIV Clinical Trials team, expanding the portfolio and linking with outpatient HIV services.You wil...Read More>>.

Betsi Cadwaladr University Health Board (BCUHB) in North Wales is seeking a Clinical Research Officer Band 5 to join the Health and Care Research Wales Research and Development team. The role supports recruitment, education and monitoring of trial...Read More>>.

NHS Greater Glasgow and Clyde (NHSGGC) is recruiting a Research Laboratory Assistant to support clinical research studies and trials at The Queen Elizabeth University Hospital. You will work within a multidisciplinary team to process samples, assi...Read More>>.